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作 者:刘英[1] 韩晓洁[1] 王树玉[1] 贾婵维[1] 任国庆[1] 余兰[1] 王丽[1]
机构地区:[1]首都医科大学附属北京妇产医院生殖中心,北京100026
出 处:《中国优生与遗传杂志》2010年第9期108-109,共2页Chinese Journal of Birth Health & Heredity
基 金:北京市科技新星基金项目(H020821200190);北京市优秀人才基金项目(20042B0301037);北京市"十百千"卫生人才培养项目
摘 要:目的观察辅助生殖技术中未受精成熟卵母细胞经钙离子载体A23187联合6-甲基嘌呤(6-DMAP)处理后的激活效果,以及激活后的胚胎发育情况。方法收集常规体外受精(IVF)及卵浆内单精子注射(ICSI)后48h仍未受精的成熟卵母细胞,经5μmol/L钙离子载体A23187处理5min,然后在2mmol/L6-DMAP中处理3h,观察原核形成情况;将激活后的卵母细胞继续体外培养3~5d,观察胚胎发育情况。结果 IVF及ICSI后未受精卵母细胞共36个,激活29个,激活率80.5%,1PN形成率31.0%,2PN形成率51.7%,多原核形成率17.2%;继续培养,卵裂率为48.3%(14/29)。15个2PN中有10个发生卵裂,2个发育至2-4细胞阶段,5个发育至5-8细胞阶段,3个发育至>8细胞阶段,最终获得2个桑葚胚。结论辅助生殖技术中未受精卵母细胞可在体外被钙离子载体A23187联合6-DMAP激活,并继续发育形成胚胎。Objective:To investigate the effect of calcium ionophore A23187 combined with 6-dimethylam inopurine(6 DMAP) on activation of human unfertilized oocytes after intracytoplasmic sperm injection(ICSI) or in intro fertilization(IVF).Methods:Unfertilized oocytes on the day of embryo transfer at 48h after ICSI or IVF were exposed to 5μmol /L calcium ionophore A23187 for 5 minutes in dark,and subsequently to 2 mmol/L 6-DMAP for 3h.The oocytes were checked for pronucleus formation at 18-20 hours after activation.Fertilized oocytes were cultured in vitro for 3 ~ 5d,the developmental potential of the activated embryos were observed.Results:29 out of 36 unfertilized oocytes were activated,and 51.7% of the activated oocytes show 2PN.Among the 10 cleaved oocyteds,2 developed to 2-4 cell stage,5 developed to 5-8 cell stage,2 developed to morular stage.Conclusion:The treatment of calcium ionophore A23187 combined with 6-DMAP could effectively activate unfertilized oocytes after IVF or ICSI 48h,and the normal fertilized oocytes could develop to embryos.
关 键 词:卵母细胞 受精失败 激活 钙离子载体A23187 6-甲基嘌呤
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